PFIZER HOSPITAL PRODUCTS GROUP ACL DRILL GUIDE— 510(k) K881378
Substantially EquivalentPfizer, Inc.
FDA 510(k) clearance K881378 for PFIZER HOSPITAL PRODUCTS GROUP ACL DRILL GUIDE, Substantially Equivalent on 1988-06-17. Applicant: Pfizer, Inc.. Device class: 1.
Clearance details
- Applicant
- Pfizer, Inc.
- Product code
- Code LXI
- Device class
- Class 1
- Regulation
- 21 CFR 878.4820
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Groton, CT, US
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